Creative Compounds, LLC Recall: Possible carbon steel foreign material (1-2mm)
United States
TerminatedClass II
- Company
- Creative Compounds, LLC
- Product
- Betaine Anhydrous, 2055kg, material packed in foil bags insi…
- Recall date
- December 15, 2025
- Terminated
- June 22, 2026
- Source
- FDA
Reason for recall
Possible carbon steel foreign material (1-2mm)
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE ANHYDROUS 98%***Distributed by Creative Compounds, LLC Scott City, Missouri USA 63780***" | Not published in this source record | 2055 kgs | Lot Code SWT2025100101 Expiration Date September 2027 |
Distribution
- 5 direct accounts located in FL
- NJ
- TX
- GA and OR
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0900-2026
- Event ID
- 99015
- Status
- Terminated
- Classification
- Class II
- Company
- Creative Compounds, LLC
- Product description
- Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE ANHYDROUS 98%***Distributed by Creative Compounds, LLC Scott City, Missouri USA 63780***"
- Quantity
- 2055 kgs
- Reason
- Possible carbon steel foreign material (1-2mm)
- Recall initiation date
- December 15, 2025
- Report date
- June 10, 2026
- Classification date
- Not published in this source record
- Termination date
- June 22, 2026
- Distribution pattern
- 5 direct accounts located in FL, NJ, TX, GA and OR
- UPC, lot, and code information
- Lot Code SWT2025100101 Expiration Date September 2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Creative Compounds, LLC
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Florida | 1 |
| New Jersey | 1 |
| Texas | 1 |
| Georgia | 1 |
| Oregon | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
